Degradation of enrofloxacin by a novel Fe–N–C@ZnO material in freshwater and seawater: Performance and mechanism
In this study, we investigated the doping of Fe–N–C with ZnO (Fe–N–C@ZnO) to enhance its performance in the reduction of biological toxicity and degradation of enrofloxacin (ENR) in seawater. The steady-state/transient fluorescence analysis and free radical quenching test indicated an extremely low...
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Published in | Environmental research Vol. 237; p. 116960 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
15.11.2023
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Subjects | |
Online Access | Get full text |
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Summary: | In this study, we investigated the doping of Fe–N–C with ZnO (Fe–N–C@ZnO) to enhance its performance in the reduction of biological toxicity and degradation of enrofloxacin (ENR) in seawater. The steady-state/transient fluorescence analysis and free radical quenching test indicated an extremely low electron–hole recombination rate and the generation of reactive oxygen species in Fe–N–C@ZnO, leading to an improvement in the energy efficiency. We compared the ENR degradation efficiencies of Fe–N–C@ZnO and ZnO using both freshwater and seawater. In freshwater, Fe–N–C@ZnO exhibited a slightly higher degradation efficiency (95.00%) than ZnO (90.30%). However, the performance of Fe–N–C@ZnO was significantly improved in seawater compared to that of ZnO. The ENR degradation efficiency of Fe–N–C@ZnO (58.87%) in seawater was 68.39% higher than that of ZnO (34.96%). Furthermore, the reaction rate constant for ENR degradation by Fe–N–C@ZnO in seawater (7.31 × 10−3 min−1) was more than twice that of ZnO (3.58 × 10−3 min−1). Response surface analysis showed that the optimal reaction conditions were a pH of 7.42, a photocatalyst amount of 1.26 g L−1, and an initial ENR concentration of 6.56 mg L−1. Fe–N–C@ZnO prepared at a hydrothermal temperature of 128 °C and heating temperature of 300 °C exhibited the optimal performance for the photocatalytic degradation of ENR. Based on liquid chromatography–mass spectrometry analysis, the degradation processes of ENR were proposed as three pathways: two piperazine routes and one quinolone route.
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•ZnO prepared at 128 °C binding with Fe–N–C shows excellent photocatalytic performance.•Fe–N–C improves ZnO's photocatalytic ability by reducing its h+ & e− recombination.•99% and 92% of ENR could be degraded by Fe–N–C@ZnO in freshwater and ASW.•ENR degradation gets three pathways: two Piperazine-Routes and one Quinolone-Route.•Fe–N–C@ZnO reduces ZnO's biological toxicity and degrades non-toxic ENR-products. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0013-9351 1096-0953 |
DOI: | 10.1016/j.envres.2023.116960 |